Revealing the Full Potential of Glycolated Mixed Ionic-Electronic Semiconductors – Symmetric Monomer Polymerization to Boost Electrochemical Transistor Performance

  • Lize Bynens
  • , Paola Mantegazza
  • , Adam Marks
  • , Yeongmin Park
  • , Arwin Goossens
  • , Stefania Moro
  • , Tyler J. Quill
  • , Garrett Lecroy
  • , Christina Cheng
  • , Arianna Magni
  • , Laurence Lutsen
  • , Jochen Vanderspikken*
  • , Simon E. F. Spencer
  • , Koen Vandewal
  • , Alberto Salleo
  • , Giovanni Costantini*
  • , Wouter Maes*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

Organic electrochemical transistors (OECTs) enable the transduction of ionic signals into electronic outputs, positioning them as ideal candidates for next-generation sensing and (bio)signal processing applications. Recent years have witnessed the development of various OECT channel materials, affording insights into structural fine-tuning to achieve optimal performance and/or stability. However, homocouplings, commonly present in alternating conjugated polymers, have largely been overlooked. This study investigates the effect of homocoupling on OECT materials by employing two synthesis methods – standard Stille polymerization and an alternative symmetric approach – to create the p-type enhancement-mode benchmark polymer pgBTTT. The impact of homocoupling, and its absence, is studied by comparing the bulk properties of the two polymers and evaluating their respective OECT metrics. The new, homocoupling-free polymer exhibits a notably improved OECT performance (μC*), mainly due to an average 3-fold increase in electronic mobility (μ).
Original languageEnglish
Pages (from-to)8383–8392
Number of pages10
JournalJournal of the American Chemical Society
Volume148
Issue number8
Early online date23 Feb 2026
DOIs
Publication statusPublished - 4 Mar 2026

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